Determining Mycotoxins and Mycotoxigenic Fungi in Food and Feed 2011
DOI: 10.1533/9780857090973.1.37
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Sample preparation and clean up in mycotoxin analysis: principles, applications and recent developments

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Cited by 13 publications
(12 citation statements)
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“…C18, C8, C6 and Florisil) is one of the conventional materials mostly used in the solid phase. Moreover, the particular stationary SPE phases, based on ion exchange, molecular recognition or immunoaffinity, are often applied in mycotoxin purification (Razzazi‐Fazeli and Reiter ). These phases considerably improve the sensitivity, selectivity and the safety of methods using products that are more efficient in the solid phase.…”
Section: Methodsmentioning
confidence: 99%
“…C18, C8, C6 and Florisil) is one of the conventional materials mostly used in the solid phase. Moreover, the particular stationary SPE phases, based on ion exchange, molecular recognition or immunoaffinity, are often applied in mycotoxin purification (Razzazi‐Fazeli and Reiter ). These phases considerably improve the sensitivity, selectivity and the safety of methods using products that are more efficient in the solid phase.…”
Section: Methodsmentioning
confidence: 99%
“…Methods for extraction of OTA from diverse biological matrices, as well as subsequent sample preparation, have simultaneously evolved. The extraction/sample preparation step is, in fact, cited as a major bottleneck in the analysis of mycotoxins [ 43 ]. Notable advances include solid-phase extraction (SPE) and, in particular, commercially available (although potentially cost prohibitive) immunoaffinity columns (IAC) for highly selective cleanup and enrichment of OTA prior to analysis [ 44 , 45 ].…”
Section: Introductionmentioning
confidence: 99%
“…Mostly mycotoxin quantitation involves chromatographic technique such as thin-layer chromatography (TLC), gas chromatography (GC) or high-performance liquid chromatography (HPLC) coupled to a photo diode array, UV-Vis or fluorescent detector, or liquid chromatography with mass spectrometry (LC-MS) or tandem mass spectrometry (LC-MS/MS)(Shephard, 2011;Spanjer, 2011). Exception to the above analytical scheme are 'dilute and shoot' methods that bypass sample clean-up but require the use of more sensitive LC-MS/MS equipment(Sulyok et al, 2007;Razzazi-fezeri and Reiter, 2011). of the fact about mycotoxins synergism in humans and animals(Speijers and Speijers, 2004;Pedrosa and Borutova, 2011) coupled with technological advancement has caused a rapid shift from single mycotoxin targeted analysis to LC-MS/MS based multimycotoxin analysis(Sulyok et al, 2006;Garon et al, 2006;Sulyok et al, 2007;Spanjer et al, 2008;Vishwanath et al, 2009;Rasmussen et al, 2010;Monbaliu et al, 2010; Ediage et al, 2011;Spanjer, 2011;Streit et al, 2013).…”
mentioning
confidence: 99%